rs79556279(T;T)

Increased risk of Behçet's disease

Magnitude
4.1Very important
Repute
Bad
On SNPedia
rs79556279(T;T)
Gene
None listed

Other genotypes of rs79556279

  1. G;GGoodcommon in complete genomicsTypical · 0.0
  2. G;TMost notableBadincreased risk of Behçet's diseaseVery important · 4.1

All about rs79556279

Notes

From SNPedia

HLA-B*51 the primary risk in Behçet's disease and rs79556279=T has the strongest association of any SNP in the HLA-B region.

References

Source and license

Adapted from rs79556279(T;T) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.